Alessandro De Luca - Mendel Inst Med Genet & Twin Res, IRCCS Casa Sollievo Sofferenza

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论文共 186 篇作者统计合作学者相似作者

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Generation of the CSSi020-A (14437) Ipsc Line from a Patient Carrying a Copy Number Variation (CNV) in the 17p11.2 Chromosome Region

Angela Maria Giada Giovenale,Elisa Maria Turco,Martina Mazzoni, Ilaria Ferrone,Barbara Torres, Laura Bernardini, Edvige Vulcano,Daniela Ferrari,Roberta Onesimo, Stefano D'Arrigo, Giuseppe Zampino,Maria Pennuto,Alessandro De Luca,Angelo Luigi Vescovi, Jessica Rosati

Stem Cell Researchpp.103544-103544, (2024)

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Primary Ciliary Dyskinesia: a Multicenter Study Assessing Genotype -Phenotype Association in Italy

Laura Petrarca, Valentina Guida, Raffaella Nenna,Alessandro De Luca, Piercarlo Poli, Maria Giulia Conti, Giuseppe Cimino, Antonella Frassanito,Enrica Mancino, Greta Di Mattia,Fabio Midulla

Paediatric bronchology (2024)

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Novel ATP2A2 Gene Mutation C.118g>a Causing Keratinocyte and Cardiomyocyte Disconnection in Darier Disease

Andrea Frustaci,Alessandro De Luca,Romina Verardo,Valentina Guida,Maria Alfarano,Camilla Calvieri,Luigi Sansone,Matteo Antonio Russo,Cristina Chimenti

BIOMEDICINES（2024）

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Breast Cancer Patient’s Postoperative Outcomes in Nipple-Sparing Mastectomy and Reconstruction with Subpectoral Implant Placement: a Single Center Experience

Alessandro De Luca,Maria Ida Amabile,Federico Frusone,Domenico Tripodi,Maria Ludovica Costanzo,Giuseppe La Torre,Marco Marcasciano,Federico Lo Torto,Massimo Monti,Massimo Vergine,Diego Ribuffo

GLAND SURGERYno. 7 (2024): 1164-1177

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Defining the Variant-Phenotype Correlation in Patients Affected by Noonan Syndrome with the RAF1:c.770C>T P.(ser257leu) Variant

EUROPEAN JOURNAL OF HUMAN GENETICSno. 8 (2024): 964-971

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Abdominoplasty after Massive Weight Loss. Safety Preservation Fascia Technique and Clinical Outcomes in a Large Single Series-Comparative Study

Claudio Cannistra,Eleonora Lori, Konstantinos Arapis,Gaetano Gallo,Marzia Varanese,Daniele Pironi,Alessandro De Luca,Federico Frusone,Maria Ida Amabile,Salvatore Sorrenti,Federica Gagliardi,Domenico Tripodi

Frontiers in Surgery (2024)

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External Hydrocephalus As a Prenatal Feature of Noonan Syndrome

Nader Khaleghi Hashemian,Gioia Mastromoro,Daniele Guadagnolo,Enrica Marchionni,Paola Daniele,Alessandro De Luca,Flavia Ventriglia,Lucia Manganaro,Antonio Pizzuti

EUROPEAN JOURNAL OF HUMAN GENETICS（2024）

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Loss-of-function Variants in ERF Are Associated with a Noonan Syndrome-Like Phenotype with or Without Craniosynostosis

EUROPEAN JOURNAL OF HUMAN GENETICSno. 8 (2024): 954-963

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Genitourinary Malformations As Possible Features of SETD5-related Syndrome

Arianna Di Daniele,Paola Daniele,Chiara De Luca,Federica Palumbo,Marco Tartaglia,Alessandro De Luca,Francesco Brancati

EUROPEAN JOURNAL OF HUMAN GENETICS（2024）

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